Associated Papers
A novel FLCN mutation in family members diagnosed with primary spontaneous pneumothorax.
Genc Yavuz B et al.
Molecular Genetics & Genomic Medicine, 2019
Mutation analysis of the FLCN gene in Chinese patients with sporadic and familial isolated primary spontaneous pneumothorax.
Ren HZ et al.
Clinical Genetics, 2008
Select a paper to view details